APA (7th ed.) Citation

NA, S., MA, E., AF, E., E, R., AM, B., FM, A., . . . K, A. (2025). Whole genome sequencing identifies monogenic disease in 56.1% of families with early-onset steroid-resistant nephrotic syndrome. Human genetics, 144(7), 727. https://doi.org/10.1007/s00439-025-02752-y

Chicago Style (17th ed.) Citation

NA, Soliman, et al. "Whole Genome Sequencing Identifies Monogenic Disease in 56.1% of Families with Early-onset Steroid-resistant Nephrotic Syndrome." Human Genetics 144, no. 7 (2025): 727. https://doi.org/10.1007/s00439-025-02752-y.

MLA (9th ed.) Citation

NA, Soliman, et al. "Whole Genome Sequencing Identifies Monogenic Disease in 56.1% of Families with Early-onset Steroid-resistant Nephrotic Syndrome." Human Genetics, vol. 144, no. 7, 2025, p. 727, https://doi.org/10.1007/s00439-025-02752-y.